Canonical Allele Identifier: PA916013078
Gene: C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12130
ClinVar RCV Id: RCV000012913 RCV000304426 RCV000454375 RCV001516299 RCV002496332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269386.1:p.Glu72Asp
CA121908
NM_001282457.2:c.216G>C
CA363370164
NM_001282457.2:c.216G>T